Condensation polymeric photoconductors containing pendant arylamines

ABSTRACT

Polymeric photoconductors are disclosed comprising a condensation polymer backbone containing, as repeating units, the condensation residues of (1) a diacid, and (2) an organic difunctional compound capable of undergoing condensation polymerization with said diacid, and an arylamine photoconductor group appended to at least one of said diacid or said organic difunctional compound residues. 
     A preferred polymeric photoconductor is ionic and comprises a condensation copolymer containing, in addition to the above described repeating units, the condensation residue of a second diacid containing an anionic iminodisulfonyl or sulfo group. In certain embodiments, the ionic arylamine-containing polymers are water-dispersible copolyesters. 
     The polymeric photoconductors described are useful in photoconductive compositions and elements. Electrophotographic processes employing such elements are also disclosed.

This is a division of application Ser. No. 285,235, filed July 20, 1981now U.S. Pat. No. 4,395,475.

FIELD OF THE INVENTION

This invention relates to photoconductive condensation polymerscontaining arylamine moieties pendant from the polymer backbone, and tophotoconductive compositions, elements and electrophotographic processesemploying such polymers.

The process of xerography, as disclosed by Carlson in U.S. Pat. No.2,297,691, employs an electrophotographic element comprising a supportmaterial bearing a coating of an insulating material whose electricalresistance varies with the amount of incident electromagnetic radiationit receives during an imagewise exposure. The element, commonly termed aphotoconductive element, is first given a uniform surface charge in thedark after a suitable period of dark adaptation. It is then exposed to apattern of actinic radiation which has the effect of differentiallyreducing the potential of this surface charge in accordance with therelative energy contained in various parts of the radiation pattern. Thedifferential surface charge, or electrostatic latent image, remaining onthe electrophotographic element is then developed by contacting thesurface with a suitable electroscopic marking material. Such markingmaterial, or toner, whether contained in an insulating liquid or in adry developer, is deposited on the exposed surface in accordance witheither the charge pattern or discharge pattern depending on the chargepolarity of the toner and the surface of the element. Deposited markingmaterial is either permanently fixed to the surface of the sensitiveelement by means such as heat, pressure, or solvent vapor, ortransferred to a second element to which it is similarly fixed.Likewise, the electrostatic charge pattern can be transferred to asecond element and developed there.

Various photoconductive insulating materials have been employed in themanufacture of electrophotographic elements. For example, selenium andselenium alloys deposited on a suitable support and particles ofphotoconductive zinc oxide held in a resinous, film-forming binder havefound wide application in present-day, document-copying processes.

Since the introduction of electrophotography, a great many organiccompounds, both monomers and polymers, have been evaluated for theirphotoconductive properties. As a result, a large number of organiccompounds are known to possess some degree of photoconductivity. Many ofthe organic compounds exhibit useful levels of photoconduction and havebeen incorporated into photoconductive compositions. Included among theknown organic photoconductive materials are triarylamine polymericphotoconductors as disclosed in U.S. Pat. Nos. 4,025,341 (issued May 27,1977 to N. G. Rule) 4,092,162 (issued May 30, 1978 to H. E. Wright etal.) and 3,779,750 (issued Dec. 18, 1973 to S. H. Merrill et al.). Inthese polymers, the triarylamine groups are divalently included directlyin the polymer backbone.

It is also known that photoconductive compositions can be madewater-dispersible by combining a photoconductor with an ionizablematerial. U.S. Pat. No. 3,471,625 (issued Oct. 7, 1969 to D. N. Adams etal), for example, discloses a two-component water-dispersiblephotoconductive composition comprising a photoconductor and afilm-forming addition polymer having ester, hydroxyl or carboxyl groupsto render the polymer water soluble at an alkaline pH.

There are problems, however, associated with the use of prior artionizable materials in photoconductor compositions. For example, in theinitial step of a copy process wherein a photoconductive composition isgiven a uniform charge, the ionizable material often interactsundesirably with the imposed charge. Either the photoconductor cannot becharged to a sufficiently high level to be useful, or the chargedissipates excessively in the dark from the photoconductor surface asdisclosed in U.S. Pat. No. 3,704,122 (issued Nov. 28, 1971 to N.Yamaguch, et al.). Furthermore, although the use of ionizable materialsin photoconductive compositions can provide water solubility ordispersibility, such materials do so in many instances at the sacrificeof solubility of the composition in organic solvents, as reported inU.S. Pat. No. 3,471,625 cited above. Accordingly, the successful use ofionizable materials is unpredictable and has been limited to the use ofspecific classes of polymers and separate photoconductors as set forthin U.S. Pat. Nos. 3,704,122 and 3,471,625. Neither of these patentsteach or suggest that ionizable polymers may also containphotoconductive groups.

In accord with the present invention, polymeric photoconductors areprovided comprising condensation polymers containing, as repeatingunits, the condensation residues of:

(a) a diacid, and

(b) an organic difunctional compound capable of undergoing condensationpolymerization with said diacid,

wherein at least one of said residues contains an appended arylaminephotoconductor group.

In accord with the present invention, the condensation polymers areoptionally ionic and in such an embodiment contain, as repeating units,the condensation residues of:

(a) a first diacid,

(b) a second diacid containing an anionic iminodisulfonyl or sulfogroup, and

(c) at least one organic difunctional compound capable of undergoingcondensation polymerization with said first and second diacids,

wherein at least one of said first diacid and organic difunctionalcompound residues contains said appended arylamine photoconductor group.

Further embodiments of the present invention include photoconductivecompositions comprising the defined photoconductors. The spectralresponse of these compositions can be modified through the use ofspectral sensitizing dyes such as pyrylium dyes. Photoconductivecompositions of the present invention are particularly useful inphotoconductive elements composed of a layer of the composition on anelectrically conducting support.

The present arylamine-containing polymers exhibit exceptionally highdegrees of photoconductivity. In some instances, moreover, high degreesof photoconductivity are provided without the presence of sensitizers.

Preferred ionic polymeric photoconductors of the present inventionexhibit particularly advantageous properties, yet the ioniciminodisulfonyl or sulfo groups do not inhibit the ability of thepolymer to otherwise function as a photoconductor. That is, the ionicphotoconductive polymer readily accepts in the dark and retains usefullevels of electrostatic charge, and readily dissipates such charge uponexposure to actinic radiation energy. Furthermore, the present ionicpolymers are readily rendered water-dispersible without sacrificing thedispersibility of the polymers in non-aqueous solvents. These ionicpolymers, moreover, when formulated into a photoconductive layer in anelement, are capable of excellent image resolution.

Polymeric photoconductors of the present invention are represented bythe structural formula: ##STR1## wherein π and π¹, which are the same ordifferent, are organic groups containing an arylamine which confersphotoconductivity upon polymer I; R¹ -π¹ together with G and G¹represents an organic condensation residue of a difunctional compoundcapable of undergoing condensation with organic diacids; R together withG² and G³ represents the organic condensation residue of at least onedifunctional compound capable of undergoing condensation with organicdiacids; G and G¹, which are the same or different, and G² and G³, whichare the same or different, represent --O-- or --NH--; A¹, A² and A³,which are the same or different, represent the residue of acid groupssuch as ##STR2## R²θ is an organic group which contains an anioniciminodisulfonyl or sulfo group; M⁺ is a cation such as ionic sodium,lithium, ammonium, phosphonium, potassium or hydrogen; --A³ --R³ --A³ --represents an organic diacid condensation residue; x is 0 to 100 molepercent of the total diacid content; y is 0 to about 35 mole percent ofthe total diacid content, and z is 0 to 100 mole percent of the totaldiacid content; the sum of x, y and z is 100; v is 0 to 100 mole percentof the total difunctional compound content; and v+x is at least 20.

As indicated by formula I, π and π¹ represent organic groups containinga monovalently appended arylamine photoconductor. Representativeexamples of π and π¹ include alkylenearylamine monovalently appendedgroups corresponding to the structure: ##STR3## wherein u is an integerfrom 1 to 6, preferably 1, and R⁵ and R⁶ are the same or different andrepresent alkyl, cycloalkyl, aryl or aralkyl and R⁴ represents alkylene,cycloalkylene, arylene or arylenealkylene, with the proviso that atleast one of R⁴, R⁵ and R⁶ comprises an aromatic group appended to thenitrogen atom. Preferred aryl and arylene groups include phenyl, tolyl,phenylene and tolylene. Preferably, R⁴, R⁵ and R⁶ are each aromatic.

In those instances when the arylamine photoconductor group is providedby repeating units of a difunctional compound capable of undergoingcondensation with organic diacids, the polymeric photoconductors of thepresent invention comprise one or more recurring units containing R¹ -π¹in structure I above. R¹ -π¹ together with G and G¹ represents thearylamine-containing condensation residue of an organic difunctionalcompound remaining after condensation with an organic diacid orfunctional equivalent of a diacid. R¹ is generally, therefore, a π¹-substituted organic radical having from about 2 to 40 carbon atoms,including optional non-carbon atoms. Exemplary R¹ radicals include π¹-substituted hydrocarbon radicals, such as straight and branched chainalkylene radicals (e.g., ethylene, trimethylene,2,2-dimethyl-1,3-propylene, etc.), cycloalkylene radicals (e.g.,cyclohexylene, cycloheptylene, etc.), and arylene radicals (e.g.,phenylene); and hydrocarbon-oxy-hydrocarbon radicals, such asalkyleneoxy-alkylene and alkylene-oxy-cycloalkylene-oxyalkylene.

Polymers according to Structure I also can contain the recurring unit##STR4## the condensation residue of at least one difunctional compoundcapable of undergoing condensation with organic diacids. R is generally,therefore, an organic radical having from about 2 to 40 carbon atoms,including optional non-carbon atoms. Exemplary radicals includehydrocarbon radicals, such as straight and branched chain alkyleneradicals (e.g., ethylene, trimethylene, 2,2-dimethyl-1,3-propylene,etc.), cycloalkylene radicals (e.g., cyclohexylene, cycloheptylene,etc.), and arylene radicals (e.g., phenylene); andhydrocarbon-oxy-hydrocarbon radicals, such as alkylene-oxy-alkylene andalkyleneoxy-cycloalkylene-oxy-alkylene.

Representative R² groups containing the anionic iminodisulfonyl group##STR5## or the anionic sulfo group

    --SO.sub.3.sup.θ

include one or more groups corresponding to the following structures:##STR6##

Polymeric photoconductors defined herein comprise, when desired,additional repeating units for any desired purpose such as varyingsolubility, charge control, compatibility with other components,adhesion, and toughness. Accordingly, the present polymers includeoptional repeating units represented, for example, by ##STR7## informula I which signifies one or more organic diacid condensationresidues. Accordingly, representative R³ groups include unsubstitutedand substituted alkylene, arylene, arylenealkylene, cycloalkylene,heterocyclic groups and ethylenically unsaturated groups.

In a preferred embodiment of the present invention, polyesterphotoconductors are provided comprising condensation polymerscontaining, as repeating units, the condensation residues of:

(a) a dicarboxylic acid, and

(b) an organic diol capable of undergoing condensation polymerizationwith said dicarboxylic acid, wherein at least one of said residuescontains an appended arylamine photoconductor group.

In the preferred embodiment, the arylamine-containing polyesters areoptionally ionic and contain in this embodiment, as repeating units, thecondensation residues of:

(a) a first dicarboxylic acid,

(b) a second dicarboxylic acid containing an anionic iminodisulfonyl orsulfo group, and

(c) at least one organic diol capable of undergoing condensationpolymerization with said first and second dicarboxylic acids,

wherein at least one of said first dicarboxylic acid and organic diolresidues contains an appended arylamine photoconductor group.

Polyester photoconductors of the present invention are accordinglyrepresented by the structural formula: ##STR8## wherein R, R¹, R², R³,M⁺, π, π¹, x, y, z and v are as defined with respect to structure Iabove.

In the preferred polyesters according to the present invention, thesecond dicarboxylic acid units, designated in structure IX as, ##STR9##can comprise residues of various conventional dicarboxylic acids such asphthalic acids, isophthalic acids, terephthalic acids andcyclohexanedicarboxylic acids. Bis-benzoic acids comprising benzoic acidmoieties linked symmetrically about other groups such as iminodisulfonylanionic groups are also advantageously employed. In each instance, ofcourse, the repeating unit contains an anionic iminodisulfonyl or sulfogroup and the M⁺ counterion.

Exemplary preferred dicarboxylic acids having an anionic iminodisulfonylgroup include

3,3'-[(sodioimino)disulfonyl]dibenzoic acid;

3,3'-[(potassioimino)disulfonyl]dibenzoic acid;

3,3'-[(lithioimino)disulfonyl]dibenzoic acid;

4,4'-[(lithioimino)disulfonyl]dibenzoic acid;

4,4'-[(sodioiminio)disulfonyl]dibenzoic acid;

4,4'-[(potassioimino)disulfonyl]dibenzoic acid;

3,4'-[(lithioimino)disulfonyl]dibenzoic acid;

3,4'-[(sodioimino)disulfonyl]dibenzoic acid;

4,4'-[(potassioimino)disulfonyl]dinaphthoic acid;

5-[N-potassio-N-(4-tolylsulfonyl)sulfamoyl]isophthalic acid andfunctional derivatives thereof. These and other dicarboxylic acids aredisclosed in U.S. Pat. No. 3,546,180 of Caldwell et al. issued Dec. 8,1970, and U.S. Pat. No. 3,929,489 of Arcesi et al. issued Dec. 30, 1975,the disclosures of which are incorporated herein by reference.

Preferred dicarboxylic acids having an anionic sulfo group include5-sodiosulfoisophthalic acid, 5-(4-sodiosulfophenoxy)isophthalic acid,5-(3-sodiosulfopropoxy)isophthalic acid,5-sodiosulfo-1,3-cyclohexanedicarboxylic acid and5-(4-sodiosulfocyclohexyloxy)-1,3-cyclohexanedicarboxylic acid andfunctionally equivalent derivatives thereof.

Considering all components, in a preferred photoconductive polyesteraccording to formula IX above, π contains triphenylamine ordi-p-tolylphenylamine, ##STR10## is derived from an organic diolselected from the group consisting of alkylenediol,di(hydroxyalkyl)cyclohexane and di(hydroxyalkoxy)cyclohexane; ##STR11##is derived from an aromatic dicarboxylic acid such as phthalic acid,isophthalic acid or terephthalic acid; and ##STR12## comprises either ananionic iminodisulfonyl or anionic sulfo group linked to the residue ofan organic dicarboxylic acid selected from the group consisting ofphthalic acids, isophthalic acids, terephthalic acids, bis(benzoicacids) or cyclohexanedicarboxylic acids; and x is from about 20 to about65 mole percent, z is 0 to about 70 mole percent, y is from about 10 toabout 35 mole percent, and v is 0.

Polymers pursuant to the present invention are readily dispersible incommon solvents such as dichloroethane. In certain of the preferredpolyesters water-dispersibility is provided by employing a molarpercentage (y in polyester IX) of the ionic diacid repeating unit thatis sufficient to confer water-dispersibility on polyester IX. In thisregard, water-dispersibility signifies that the resulting polyester willform a stable aqueous composition comprising a dispersion or solutioncontaining at least 3 weight percent of the polyester for at least twomonths, usually six months or more, with essentially no visible signs ofagglomeration or crystallization. Preferred water-dispersiblephotoconductive polyesters of the present invention that form suchaqueous compositions correspond to structure IX wherein y is from about10 to about 30, and x is from about 40 to about 60, and v is 0.

As shown in connection with structure I above, π and π¹ groupscontaining arylamine photoconductive groups are appended to a diacidresidue or difunctional organic compound residue in the definedphotoconductive polymers. Such arylamine groups are attached to thediacid side of the polymer, for example, by basic condensation of anarylamine having an aldehyde substituent with an active methylene of adiacid radical to produce an unsaturated bond joining the photoconductorto the diacid radical. The unsaturated bond is thereafter reduced byhydrogenation over a palladium/charcoal catalyst. Schematically, thepreparation of the arylamine-containing group is shown as follows:##STR13## wherein A¹, R⁴, R⁵ and R⁶ are defined above. ##STR14##

The arylamine photoconductor group is attached to the diacid precursorof the defined polymer followed by polycondensation of the diacidcomponent with the other appropriate condensation polymer components.Alternatively, the arylamine is attached to the diacid component of apreformed polymer. The alternative method is preferred in the event thathigh molecular weight polymers are desired.

When it is desirable to append the arylamine to a difunctional organiccompound, particularly a diol, that is capable of undergoingcondensation polymerization with the diacid precursors in the definedpolymers, dicarboxylic acids containing the pendant arylamine arechemically reduced to yield the corresponding diol. Attachment of thearylamine to organic diamines or hydroxyamines can be carried out byknown techniques such as by attaching the arylamine to an organiccompound already having the amine or hydroxyamine function-ality.Alternatively, an arylamine can be treated to form the diamine orhydroxyamine functionality.

The polymers described herein, with or without pre-attached arylaminephotoconductive groups, are prepared by procedures well known in the artfor making linear condensation polymers, particularly interfacial,solution or ester interchange procedures, the latter being preferred forpolyesters. Reaction times are governed by the inherent viscositydesired for the resulting polymer. For purposes of illustration,examplary procedures for the preparation of polyesters (Structure IX)are described hereinafter.

When employing interfacial procedures, polymerization is carried out insuitable halogenated solvents, such as methylene chloride, chloroform,dichloromethane, or propylene dichloride. Reaction temperatures aregoverned by maintenance of a practical rate of reaction and the boilingpoint of the solvent, with a range of 10° to 40° C. being suitable.

Solution polymerization procedures can be carried out by condensingsuitable acid halides, such as terephthaloyl, isophthaloyl, orcyclohexanedicarboxylic acid chlorides, with the desired diols in asuitable solvent, in the presence of a suitable acid acceptor, such aspyridine, triethylamine, or tripropylamine. The acid acceptor can beemployed in excess to serve as the solvent.

A preferred mode of preparing the polyesters disclosed herein is theester interchange procedure either by melt or powder process, andpreferably by the melt process. The diols and the carboxylates areheated to a melt on an approximately equal molar basis and treated witha transesterification catalyst such as alkali or alkaline earth metalcarbonates, oxides, hydroxides, hydrides, and alkoxides; or compounds ofa Group IVB metal of the Periodic Table, such as tetraisopropylorthotitanate, butyl titanate, organo-metallic halides, and complexalkoxides such as NaHTi(OC H₉)₂. As a practical matter, it is frequentlydesirable to utilize an excess of up to about 80 molar percent of thediol component in the reaction mixture. Low boiling alcohols are removedby distillation during polymerization.

The condensation polymers described herein exhibit an inherent viscosityof from about 0.10 to about 0.50 and preferably from 0.1 to 0.4 asmeasured at 25° C. at a concentration of 0.25 g/deciliter in a 1:1mixture of phenol and chlorobenzene.

The polymers described herein have a glass transition temperature withinthe range of about 30° C. to about 90° C. as determined by differentialscanning colorimetry as disclosed in "Techniques and Methods of PolymerEvaluation", Vol. 2, Marcel Dekker, Inc., N.Y., 1970.

The structures of representative photoconductive polyesters containingappended arylamine photoconductors as described herein are shown inTable I below (mole percentages set forth by parenthesis indicate aseparate polymer of the structure shown):

                                      TABLE I                                     __________________________________________________________________________     ##STR15##                                                                    2                                                                              ##STR16##                                                                    3                                                                              ##STR17##                                                                    4                                                                              ##STR18##                                                                    5, 6                                                                           ##STR19##                                                                     ##STR20##                                                                    7, 8                                                                           ##STR21##                                                                     ##STR22##                                                                    9, 10, 11, 12                                                                  ##STR23##                                                                     ##STR24##                                                                    13                                                                             ##STR25##                                                                     ##STR26##                                                                    14                                                                             ##STR27##                                                                     ##STR28##                                                                    15                                                                             ##STR29##                                                                     ##STR30##                                                                    16                                                                             ##STR31##                                                                     ##STR32##                                                                    17                                                                             ##STR33##                                                                     ##STR34##                                                                    18                                                                             ##STR35##                                                                     ##STR36##                                                                    __________________________________________________________________________

The utility of the present polymeric photoconductors extends generallyto those areas in which a photocondutive component is desirable such asin electrophotography. In electrophotography, compositions comprisingthe polymeric photoconductors are applied as layers to electroconductingsupports to form electrophotographic elements. Alternatively, layerscontaining the present polymeric photoconductors can be employed to formmultilayer electrophotographic elements with or without additionallayers containing other photoconductors. In such multilayerelements--often referred to as multiactive elements--one photoconductorlayer functions as a charge generation layer while a secondphotoconductor layer functions as a transport layer for the generatedcharge. The present polymeric photoconductors are useful in such chargegeneration or charge transport layers.

The polymeric photoconductive materials of the invention are employed inphotoconductive compositions and layers with or without a separatebinder and with or without sensitizing addenda and/or additionaloptional photoconductors. Generally, because of the film-formingproperties of a polymeric material, a binder is not required. In suchcase, the photoconductor is dissolved or dispersed in a suitable solventand coated on a support to form a self-supporting film layer.

Solvents of choice for preparing coating compositions of the presentinvention include organic solvents such as benzene, toluene, acetone,2-butanone, chlorinated hydrocarbons such as methylene chloride andethylene chloride, ethers such as tetrahydrofuran or mixtures of thesesolvents. In those instances where water-dispersible ionic polymericphotoconductors are employed, water is employed as solvent to form anaqueous coating composition.

In preparing the coating composition useful results are obtained wherethe photoconductor substance is present in an amount equal to at leastabout 1 weight percent of the coating composition (on a solvent-freebasis). The upper limit in the amount of photoconductor substancepresent is not critical. As indicated previously, the polymericmaterials of the present invention do not require a separate binder inorder to obtain a self-supporting coating on the support. In those caseswhere a separate binder is employed, it is normally desirable that thephotoconductor substance be present in an amount of from about 1 weightpercent of the coating composition to about 99 weight percent of thecoating composition. A preferred weight range for the photoconductorsubstance in the coating composition is from about 10 weight percent toabout 60 weight percent.

Coating thicknesses of the photoconductive composition on a support canvary widely. Normally a dry coating in the range of about 0.5 micron toabout 30 microns is useful for the invention.

Suitable supporting materials for electrophotographic elements of theinvention include electrically conducting supports such as paper orconventional film supports, for example, cellulose acetate, cellulosenitrate, polystyrene, poly(ethylene terephthalate), poly(vinyl acetal),polycarbonate and related films having a conductive layer thereon. Auseful conducting support is prepared by coating a transparent filmsupport material with a layer containing a semiconductor such as cuprousiodide dispersed in a resin. Suitable conducting coatings are alsoprepared from the sodium salt of a carboxyester lactone of maleicanhydride-vinyl acetate copolymer. Such conducting layers and methodsfor their optimum preparation and use are disclosed in Minsk U.S. Pat.No. 3,007,901 issued Nov. 7, 1961; Trevoy U.S. Pat. No. 3,245,833 issuedApr. 12, 1966; Sterman et al. U.S. Pat. No. 3,262,807 issued July 26,1966; etc. Additional useful conductive layers include carbon-containinglayers such as conductive carbon particles dispersed in a resin binder.Metal coated papers; metal-paper laminates; metal foils such as aluminumfoil; metal plates such as aluminum, copper, zinc, brass and galvanizedplates; as well as vapor deposited metal layers such as silver, nickelor aluminum deposited on conventional film supports are also useful asare conductive or conductor-coated glasses.

Sensitizing compounds, if desired for use with the photoconductiveelements of the present invention, are selected from a wide variety ofmaterials known in the art as sensitizers for organic photoconductors.Especially preferred sensitizers are pyrylium dye salts includingthiapyrylium dye salts and selenapyrylium dye salts disclosed inVanAllan et al. U.S. Pat. No. 3,250,615. Useful other materials includethe spectral sensitizers in any one of U.S. Pat. Nos. 3,705,913;3,615,416; 3,589,897; 3,958,991; 3,796,573 and 3,597,196, as well asboron diketonate dyes as disclosed in Daniel et al U.S. Pat. No.3,567,439.

The amount of sensitizer that is added to a photoconductive compositionof the invention to give effective increases in speed varies widely. Theoptimum concentration will vary with the specific photoconductor andsensitizing compound used. In general, substantial speed gains areobtained where an appropriate sensitizer is added in a concentrationrange from about 0.0001 to about 10 weight percent or more heated on theweight of the coating composition. Normally, sensitizers are added tothe coating composition in an amount of 0.005 to about 5.0 weightpercent of the total coating composition.

A preferably preferred electrophotographic element employing thepolymeric photoconductors according to the invention comprises a papersupport having an electroconducting polymeric layer on each side of thepaper support. A brightening layer composed of TiO₂ is coated on one ofthe electroconducting polymeric layers and a photoconductive layercomprising a water-dispersible ionic polymeric photoconductor asdescribed herein coated from an aqueous coating composition over theTiO₂ containing layer.

The following procedures and examples are provided to illustrate thepreparation and utility of polymeric photoconductors of the presentinvention.

Polymerization Procedure

All of the polymers described in Table I can be synthesized by thestandard high temperature melt condensation procedure described below.Polyesters are described for purposes of illustration.

A polymerization flask was charged with the appropriate diols anddiesters. The flask was equipped with a Vigreaux condenser. Thecondenser was fitted with a nitrogen inlet tube and gas flushed throughthe system at 40 ml/min. The flask was immersed in a 235° C. salt bathto just below the stoppered side arm. When the chemical mixture became ahomogeneous melt, one drop of tetraisopropyl orthotitanate was added asa catalyst.

The volatiles were distilled at 235° C. and at atmospheric pressure for4 hrs. The condenser and inlet tube were replaced with a stainless steelstirrer attached so as to be vacuum tight. A vacuum was drawn to about0.05 mm Hg, the polymer stirred at 200 rpm and the torque applied by themelt to the stirrer measured. When the torque indicated the desireddegree of polymerization, the stirring and vacuum were stopped and thepolymerization flask removed from the bath as quickly as possible. Thepolymerization flask was immersed in liquid nitrogen and the flaskbroken away from the solidified glassy polymer.

Condensation of the Malonate-Containing Polymers with the ArylaminesContaining an Aldehyde Substituent

This illustrates the attachment of the arylamine photoconductive groupto a preformed polyester. The preparation of polyester 16 in Table I isdescribed to exemplify this method. Polyesters 15 and 17 were alsoprepared by this method with appropriate modification of the reactantsset forth below.

A one-liter, three-necked, round-bottom reaction flask equipped with astirrer, thermometer, and condenser was charged with 27.7 g of polymer19 below and 300 ml of dry 1,2-dichloroethane. ##STR37## In 50 ml of dry1,2-dichloroethane was dissolved 5.33 g of diphenylaminobenzaldehyde.The latter solution and 0.1 gm of piperidine were added to the reactionflask. After thorough mixing, 2 g of 4 A molecular sieves were added,and the reaction was stirred for four days. The reaction mixture wasfiltered and the 1,2-dichloroethane was evaporated leaving a polymericresidue. The residue was extracted with acetonitrile to eliminateunreacted diphenylaminobenzaldehyde. The yield was 18.8 g of polyester16.

Condensation of Diethyl Malonate with a Triarylamine containing anAldehyde Substituent

This illustrates the attachment of the triarylamine photoconductivegroup to a malonate diacid. The resulting malonate-photoconductor diacidwas then polymerized as described above with appropriate glycols andother diacids to produce polyesters 5-14 in Table I.

A five-liter, three-necked, round-bottom flask equipped with stirrer,thermometer, Dean Stark trap, and condenser was charged with 391.8 g ofdi-p-tolylaminobenzaldehyde, 208 g diethyl malonate, 11 ml ofpiperidine, 13 ml of acetic acid, and 1500 ml of toluene. The reactionsolution was refluxed for 6 hours, and during this time 32 ml of waterwas collected. The reaction was cooled and the toluene was evaporated.The product was taken up in 900 ml of ethanol, and the ethanol wasslowly reduced in volume by evaporation. The crystalline product wascollected, and had a melting point of 99°-105° C. The product wasrecrystallized again from ethanol, dried, and had a melting point of104°-106° C. The yield was 494 g. The condensation product, diethyl4-[N,N-di-p-tolylamino]benzylidenemalonate, was reduced using palladiumover charcoal as the catalyst.

Examples 1-3

These examples illustrate the solvent coating of ionic polyesters of thepresent invention to form photoconductive layers on a conductive filmsupport and the resulting photodischarge characteristics of thephotoconductive layers.

The ionic polyester 6 from Table I was dissolved in tetrahydrofuran(THF) at 20% solids. The solution was coated onto 0.4 O.D. (opticaldensity) nickel-coated poly(ethylene terephthalate) support to give adry coating of approximately 6.5μ thick. Another solution was preparedand coated as above, except 0.5% of the following sensitizer was added:##STR38## A third solution was prepared and coated as above exceptpolyester 10 replaced polyester 6 to a coating thickness of 7μ, anddichloroethane replaced THF as solvent.

The resulting photoconductive layers were charged to an initial chargingpotential (V_(o)), exposed to a 350 nm monochromatic light source, andthe photodischarge measurements of the layers were determined as thenumber of ergs/cm² required to dissipate the charge to 1/2V_(o).

The results of the photodischarge measurements are listed in Table II.

                  TABLE II                                                        ______________________________________                                        Photodischarge Sensitivity of                                                 Sensitized Ionic Polyester Photoconductors                                    (Positive Charging-Front Surface Exposure)                                                                   Photodischarge                                                      Charging  to 1/2 V.sub.o at                                                   Potential,                                                                              λ = 350 nm                              Example Polymeric film                                                                             Vo (volts)                                                                              [ergs/cm.sup.2 ]                               ______________________________________                                        1       Polyester 6  +441      56                                             2       Polyester 6 +                                                                              +375      33                                                     sensitizer                                                            3       Polyester 10 +500      98                                             ______________________________________                                    

Examples 4-8

These examples demonstrate the aqueous coating of ionic polyesters ofthe present invention to form photoconductive layers on a film supportand the resulting electrical properties (positive or negative chargingmodes) of the photoconductive layers.

Various ionic polyesters from Table I were dispersed in water at 20-25%solids and coated on the nickel coated support described in Examples 1-3above. The dry coating thickness ranged from 6.5μ to 7μ.

The elements produced were evaluated for saturation potential (V_(sat))and time constants (τ) of dark decay using a Monroe ElectrostaticVoltmeter, a strip chart recorder in conjunction with a corona charger,and a rotatable metal cylinder on which the sample was mounted.Continuous charging (positive and negative) of the sample was carriedout until the voltmeter indicated no further increase in surfacepotential. The charger was then shut off, and the output of thevoltmeter recorded as it indicated the dark decay of the surfacepotential of the sample. Dark decay was recorded until the potential haddecreased to 1/3 of V_(sat), defining the time constant of decay, τ.

The results of these measurements are shown in Table III below.

                  TABLE III                                                       ______________________________________                                        Dark Decay and Dark Decay Properties                                          Of Ionic Polyester Photoconductor Films                                                                   V.sub.sat                                                                           (V.sub.sat →                         Example   Polymer  RH       (volts)                                                                             (sec.) 1/3 V.sub.sat)                       ______________________________________                                        4          9       50%      +560  +280                                                                    -560  -280                                        5         13       50%      +440  +175                                                                    -440  -175                                        6          8       50%      +450  +260                                                                    -450  -260                                        7         .sup. 11.sup.a                                                                         35%      +620  +900                                                                    -580  -900                                        8         .sup. 12.sup.a                                                                         35%      +820  +900                                                                    -800  -900                                        ______________________________________                                         .sup.a Films dark adapted for 24 hours prior to charging.                

Examples 9-13

These examples illustrate electrophotographic elements composed ofconducting paper supports coated with aqueous dispersions containing anionic polyester of the present invention. The electrical properties andphotodischarge characteristics of the resulting elements are also setforth.

Polyester 12 from Table I was combined with 70° C. water at 20% solids,and dispersed with a paddle stirrer. To the aqueous dispersion was added0.5 wt/% of the following water-soluble sensitizer: ##STR39## Theaqueous dispersion was machine coated onto a conductive paper support.This support comprises a TiO₂ coated paper substrate coated on the backside with a conductive layer of a dispersed clay including a conductiveclay (Bentonite® Clay, an aluminum silicate) dispersed in apoly(styrene-cobutadiene) latex. The coatings were made to produce arange of polymer coverages. The electrical properties of thesephotoconductive paper coatings are listed in Table IV.

                                      TABLE IV                                    __________________________________________________________________________    Dark Charging, Dark Decay and Photosensitivity of                             Ionic Polyester Photoconductor Coated Papers                                  Dry              V.sub.sat                                                                             τ                                                                             (V.sub.sat →                                                                  Photodischarge (+500                      Coverage   Thickness                                                                           (volts) (sec)                                                                             1/3 V.sub.sat                                                                     RH Volts to 250 volts)                       Example                                                                            g/m.sup.2                                                                           (microns)                                                                           +   -   +   -   (%)                                                                              at λ = 350 nm                      __________________________________________________________________________     9   12.5  14.8  >1000                                                                             >1000                                                                             >1200                                                                             >1200                                                                             55 94 ergs/cm2                               10   15.0  11.0    780                                                                               860                                                                             >1200                                                                             >1200                                                                             55 88 ergs/cm2                               11   17.0  13.2    750                                                                               840                                                                             >1200                                                                             >1200                                                                             55 --                                        12   19.0  17.0  >1000                                                                               920                                                                             >1200                                                                             >1200                                                                             55 --                                        13   10.0   9.0  >1000                                                                             >1000                                                                             >1200                                                                             >1200                                                                             55 78 ergs/cm2                               __________________________________________________________________________

Examples 14-17

These examples illustrate spectral sensitization of ionic polymericphotoconductors of the present invention into the visible region of thespectrum using appropriate spectral sensitizing dyes.

To separate solutions of the polyester 12 dissolved in dichloromethane(10% by weight, polyester) the following spectral sensitizing dyes wereadded at a concentration of 2%, by weight. The resulting solutions werecoated on 0.4 O.D. nickel coated poly(ethylene terephthalate) supports,and dried 16 hours at 60° C. ##STR40## The photodischargecharacteristics in ergs/cm² of the prepared layers was determined forvarious wavelengths of light in the visible portion of the spectrum.Results are shown in Table V

                  TABLE V                                                         ______________________________________                                        Photosensitivity of                                                           Visibly Sensitized Ionic Polyester Photoconductors                                   Dry                       Photo                                               Layer             Charging                                                                              discharge                                                                             Wave                                        Thick-   Sensitiz-                                                                              Potential                                                                             Vo- → 1/2 Vo                                                                   length                               Example                                                                              ness μ                                                                              ing Dye  (Vo)    (ergs/cm.sup.2)                                                                       (nm)                                 ______________________________________                                        14     10       S-1      +425    131     546                                                           +754    131     546                                                           -233    626     546                                                           -292    583     546                                  15     10       S-2      +483    92      430                                                           +625    95      430                                                           +650    84      430                                                           -183    178     430                                                           -258    167     430                                                           -375    130     430                                  16     8        S-3      +483    59      565                                                           +600    68      565                                                           +621    73      565                                                           -242    215     565                                                           -525    137     565                                  17     9        S-4      +408    418     642                                                           -433    1009    642                                                           -542    735     642                                                           -642    649     642                                  ______________________________________                                    

Example 18

This exemplifies the use of the element described in Example 9 above ina copy process to produce a toned visible image.

An electrophotographic copying device was assembled containing agrid-controlled corona charger, a vacuum platten to accept a 70 mm widestrip, an insulative glass with an attached negative test target, atungsten lamp controlled by a timer, and an immersion liquid tonerstation. The element from Example 13 was charged to +500 volts, exposedfor five seconds and then developed for one second using Recordak® 12NNegative Liquid Toner (available from Eastman Kodak Company, Rochester,New York). The element was also charged to +300 volts, and then exposed,and developed as above. Very sharp, well-resolved images were obtainedin both cases.

The invention has been described in detail with particular reference topreferred embodiments thereof, but it will be understood that variationsand modifications can be effected within the spirit and scope of theinvention.

What is claimed is:
 1. A polymeric photoconductor comprising acondensation polymer containing, as repeating units, the condensationresidues of:(a) a diacid, and (b) an organic difunctional compoundcapable of undergoing condensation polymerization with saiddiacid,wherein at least one of said residues contains an appendedarylamine photoconductor group.
 2. The polymeric photoconductor of claim1 wherein the residue of said organic difunctional compound containssaid appended arylamine.
 3. The polymeric photoconductor of claim 1wherein the residue of said diacid contains said appended arylamine. 4.The polymeric photoconductor of claim 2 or 3 wherein said arylamine is atriarylamine.
 5. An ionic polymeric photoconductor comprising acondensation polymer containing, as repeating units, the condensationresidues of:(a) a first diacid, (b) a second diacid containing ananionic iminodisulfonyl or sulfo group, and (c) at least one organicdifunctional compound capable of undergoing condensation polymerizationwith said first and second diacids,wherein at least one of said firstdiacid and organic difunctional compound residues contains said appendedarylamine photoconductor group.
 6. The ionic polymeric photoconductor ofclaim 5 wherein the residue of said organic difunctional compoundcontains said appended arylamine.
 7. The ionic polymeric photoconductorof claim 5 wherein the residue of said first diacid contains saidappended arylamine.
 8. The ionic polymeric photoconductor of claim 6 or7 wherein said arylamine is a triarylamine.
 9. A polymericphotoconductor having the structure ##STR41## wherein π and π¹, whichare the same or different, are organic groups containing an arylaminewhich confers photoconductivity upon the polymer; R¹ --π¹ together withG and G¹ represents an arylamine-containing organic condensation residueof a difunctional compound capable of undergoing condensation withorganic diacids; R together with G² and G³ represents at least oneorganic condensation residue of a difunctional compound capable ofundergoing condensation with organic diacids; G and G¹, which are thesame or different, and G² and G³, which are the same or different,represent --O-- or --NH--; A¹, A² and A³, which are the same ordifferent, represent the condensation residues of acid groups; R²θ is anorganic group which contains an anionic iminodisulfonyl or sulfo group;M⁺ is a cation; --A³ --R³ --A³ represents an organic diacid condensationresidue; x is 0 to 100 mole percent of the total diacid content; y is 0to about 35 mole percent of the total diacid content; z is 0 to 100 molepercent of the total diacid content; the sum of x, y and z is 100; v is0 to 100 mole percent of the total difunctional compound content; andv+x is at least
 20. 10. A polymeric photoconductor as in claim 9 whereinπ and π¹ have the structure ##STR42## wherein u is an integer from 1 to6; R⁵ and R⁶ are the same or different and represent alkyl, cycloalkyl,aryl or aralkyl; R⁴ is alkylene, cycloalkylene, arylene orarylenealkylene; at least one of R⁴, R⁵ and R⁶ comprises an aromaticgroup appended to the nitrogen atom; R³ is an alkylene, arylene,arylenealkylene, cycloalkylene, heterocyclic or an ethylenicallyunsaturated group; and A¹, A² and A³ are ##STR43##
 11. A polymericphotoconductor as in claim 10 wherein R⁴, R⁵ and R⁶ each comprise anaromatic group appended to the nitrogen atom.
 12. A polymericphotoconductor as in claim 10 wherein R⁴ is phenylene, R⁵ and R⁶ areeach phenyl or tolyl, u is 1, and v is
 0. 13. A polymeric photoconductorof claim 10, 11 or 12 wherein R² is selected from the group consistingof: ##STR44##
 14. A polymeric photoconductor comprising a polyestercontaining, as repeating units, the condensation residues of:(a) adicarboxylic acid, and (b) an organic diol capable of undergoingcondensation polymerization with said dicarboxylic acid, wherein atleast one of said residues contains an appended arylamine photoconductorgroup.
 15. The polyester of claim 14 wherein the residue of said organicdiol contains said appended arylamine.
 16. The polyester of claim 14wherein the residue of said dicarboxylic acid contains said appendedarylamine.
 17. The polyester of claim 15 or 16 wherein said arylamine isa triarylamine.
 18. An ionic polymeric photoconductor comprising apolyester containing, as repeating units, the condensation residuesof:(a) a first dicarboxylic acid, (b) a second dicarboxylic acidcontaining an anionic iminodisulfonyl or sulfo group, and (c) at leastone organic diol capable of undergoing condensation polymerization withsaid first and second dicarboxylic acids,wherein at least one of saidfirst dicarboxylic acid and organic diol residues contains an appendedarylamine photoconductor group.
 19. A polymeric photoconductor havingthe structure ##STR45## wherein π and π¹, which are the same ordifferent, are organic groups containing an arylamine which confersphotoconductivity upon the polymer; ##STR46## is the condensationresidue of an arylamine-containing organic diol having from about to 2about 40 carbon atoms; --O--R--O-- is the condensation residue of atleast one organic diol having from about 2 to about 40 carbon atoms; R²θis an organic group which contains an anionic iminodisulfonyl or sulfogroup; M⁺ is a cation; ##STR47## represents an organic dicarboxylic acidcondensation residue; x is 0 to 100 mole percent of the totaldicarboxylic acid content; y is 0 to about 35 mole percent of the totaldicarboxylic acid content; z is 0 to 100 mole percent of the totaldicarboxylic acid content; the sum of x, y and z is 100; v is 0 to 100mole percent of the total diol content; and v+x is at least
 20. 20. Apolymeric photoconductor as in claim 19 wherein π and π¹ have thestructure: ##STR48## wherein u is an integer from 1 to 6; R⁵ and R⁶ arethe same or different and represent alkyl, cycloalkyl, aryl or aralkyl;R⁴ is alkylene, cycloalkylene, arylene or arylenealkylene; at least oneof R⁴, R⁵ and R⁶ comprises an aromatic group appended to the nitrogenatom; and R³ is an alkylene, arylene, arylenealkylene, cycloalkylene,heterocyclic or an ethylenically unsaturated group.
 21. A polymericphotoconductor as in claim 20 wherein R⁴, R⁵ and R⁶ each comprise anaromatic group appended to the nitrogen atom.
 22. A polymericphotoconductor as in claim 20 wherein R⁴ is phenylene, R⁵ and R⁶ areeach phenyl or tolyl, u is 1, and v is
 0. 23. A water-dispersiblepolymeric photoconductor as in claim 20, 21 or 22 wherein v is 0, x isfrom about 40 to about 60 mole percent, and y is from about 10 to about30 mole percent.
 24. A polymeric photoconductor of claim 23 wherein R²is selected from the group consisting of ##STR49##
 25. A polymericphotoconductor of claim 20, 21 or 22 wherein the repeating unit##STR50## is the condensation residue of a dicarboxylic acid selectedfrom the group consisting of 3,3'-[(sodioimino)disulfonyl]dibenzoicacid; 3,3'-[(potassioimino)disulfonyl]dibenzoic acid;3,3'-(lithioimino)disulfonyl]dibenzoic acid;4,4'-[(lithioimino)disulfonyl]dibenzoic acid;4,4'-[(sodioimino)disulfonyl]dibenzoic acid;4,4'-[(potassioimino)disulfonyl]dibenzoic acid;3,4'-[(lithioimino)disulfonyl]dibenzoic acid;3,4'-[(sodioimino)disulfonyl]dibenzoic acid;4,4'-[(potassiomino)disulfonyl]dinaphthoic acid;5-[N-potassio-N-(4-tolylsulfonyl)sulfamoyl]isophthalic acid,5-sodiosulfoisophthalic acid, 5-(4-sodiosulfophenoxy)isophthalic acid,5-(3-sodiosulfopropoxy)isophthalic acid, and5-(4-sodiosulfocyclohexyloxy)-1,3-cyclohexanedicarboxylic acid.
 26. Awater-dispersible polymeric photoconductor as in claim 23 wherein therepeating unit ##STR51## is the condensation residue of a dicarboxylicacid selected from the group consisting of3,3'-[(sodioimino)disulfonyl]dibenzoic acid;3,3'-[(potassioimino)disulfonyl]dibenzoic acid;3,3'-[(lithioimino)disulfonyl]dibenzoic acid;4,4'-[(lithioimino)disulfonyl]dibenzoic acid;4,4'-[(sodioimino)disulfonyl]dibenzoic acid;4,4'-[(potassioimino)disulfonyl]dibenzoic acid;3,4'[(lithioimino)disulfonyl]dibenzoic acid;3,4'-[(sodioimino)disulfonyl]dibenzoic acid;4,4'[(potassiomino)disulfonyl]dinaphthoic acid;5-[N-potassio-N-(4-tolylsulfonyl)sulfamoyl]isophthalic acid,5-sodiosulfoisophthalic acid, 5-(4-sodiosulfophenoxy)isophthalic acid,5-(3-sodiosulfopropoxy)isophthalic acid, and5-(4-sodiosulfocyclohexyloxy)-1,3-cyclohexanedicarboxylic acid.
 27. Aphotoconductive composition comprising a condensation polymercontaining, as repeating units, the condensation residues of:(a) adiacid, and (b) an organic difunctional compound capable of undergoingcondensation polymerization with said diacid,wherein at least one ofsaid residues contains an appended arylamine photoconductor group. 28.The composition of claim 27 wherein said arylamine is a triarylamine,said composition further comprising a spectral sensitizer.
 29. An ionicphotoconductive composition comprising a condensation polymercontaining, as repeating units, the condensation residues of:(a) a firstdiacid, (b) a second diacid containing an anionic iminodisulfonyl orsulfo group, and (c) at least one organic difunctional compound capableof undergoing condensation polymerization with said first and seconddiacids,wherein at least one of said first diacid and organicdifunctional compound residues contains said appended arylaminephotoconductor group.
 30. The ionic composition of claim 29 wherein saidarylamine is a triarylamine, said composition further comprising aspectral sensitizer.
 31. A photoconductive composition comprising(a) apolymeric photoconductor having the structure ##STR52## wherein π andπ¹, which are the same or different, are organic groups containing anarylamine which confers photoconductivity upon the polymer; R¹ -π¹together with G and G¹ represents an arylamine-containing organiccondensation residue of a difunctional compound capable of undergoingcondensation with organic diacids; R together with G² and G³ representsat least one organic condensation residue of a difunctional compoundcapable of undergoing condensation with organic diacids; G and G¹, whichare the same or different, and G² and G³, which are the same ordifferent, represent --O-- or --NH--; A¹, A² and A³, which are the sameor different, represent the condensation residues of acid groups; R²θ isan organic group which contains an anionic iminodisulfonyl or sulfogroup; M⁺ is a cation; --A³ --R³ --A³ represents an organic diacidcondensation residue; x is 0 to 100 mole percent of the total diacidcontent; y is 0 to about 35 mole percent of the total diacid content; zis 0 to 100 mole percent of the total diacid content; the sum of x, yand z is 100; v is 0 to 100 mole percent of the total difunctionalcompound content; and v+x is at least 20, and (b) a spectral sensitizer.32. A composition as in claim 31 wherein π and π¹ have the structure##STR53## wherein u is an integer from 1 to 6; R⁵ and R⁶ are the same ordifferent and represent alkyl, cycloalkyl, aryl or aralkyl; R⁴ isalkylene, cycloalkylene, arylene or arylenealkylene; at least one of R⁴,R⁵ and R⁶ comprises an aromatic group appended to the nitrogen atom; R³is an alkylene, arylene, arylenealkylene, cycloalkylene, heterocyclic oran ethylenically unsaturated group; A¹, A² and A³ are ##STR54## and saidspectral sensitizer is a pyrylium dye salt.
 33. The composition as inclaim 32 wherein R⁴ is phenylene, R⁵ and R⁶ are each phenyl or tolyl, uis 1, and v is
 0. 34. The composition of claim 32 or 33 wherein R² isselected from the group consisting of: ##STR55##
 35. A photoconductivecomposition comprising a polyester containing, as repeating units, thecondensation residues of:(a) a dicarboxylic acid, and (b) an organicdiol capable of undergoing condensation polymerization with saiddicarboxylic acid,wherein at least one of said residues contains anappended arylamine photoconductor group.
 36. The composition of claim 35wherein said arylamine is a triarylamine, said composition furthercomprising a spectral sensitizer.
 37. An photoconductive compositioncomprising a polyester containing, as repeating units, the condensationresidues of:(a) a first dicarboxylic acid, (b) a second dicarboxylicacid containing an anionic iminodisulfonyl or sulfo group, and (c) atleast one organic diol capable of undergoing condensation polymerizationwith said first and second dicarboxylic acids, wherein at least one ofsaid first dicarboxylic acid and organic diol residues contains anappended arylamine photoconductor group.
 38. A photoconductivecomposition comprising(a) a polymeric photoconductor having thestructure ##STR56## wherein π and π¹, which are the same or different,are organic groups containing an arylamine which confersphotoconductivity upon the polymer; ##STR57## is the condensationresidue of an arylamine-containing organic diol having from about to 2about 40 carbon atoms; --O--R--O-- is the condensation residue of atleast one organic diol having from about 2 to about 40 carbon atoms; R²θis an organic group which contains an anionic iminodisulfonyl or sulfogroup; M⁺ is a cation; ##STR58## represents an organic dicarboxylic acidcondensation residue; x is 0 to 100 mole percent of the totaldicarboxylic acid content; y is 0 to about 35 mole percent of the totaldicarboxylic acid content; z is 0 to 100 mole percent of the totaldicarboxylic acid content; the sum of x, y and z is 100; v is 0 to 100mole percent of the total diol content; and v+x is at least 20, and (b)a spectral sensitizer.
 39. The composition as in claim 38 wherein π andπ¹ has the structure: ##STR59## wherein u is an integer from 1 to 6; R⁵and R⁶ are the same or different and represent alkyl, cycloalkyl, arylor aralkyl; R⁴ is alkylene, cycloalkylene, arylene or arylenealkylene;at least one of R⁴, R⁵ and R⁶ comprises an aromatic group appended tothe nitrogen atom; R³ is an alkylene, arylene, arylenealkylene,cycloalkylene, heterocyclic or an ethylenically unsaturated group, andsaid spectral sensitizer is a pyrylium dye salt.
 40. The composition asin claim 39 wherein R⁴ is phenylene, R⁵ and R⁶ are each phenyl or tolyl,u is 1, and v is
 0. 41. An aqueous photoconductive compositioncontaining a water-dispersible polymeric photoconductor comprising apolymer as in claim 39 or 40 wherein v is 0, x is from about 40 to about60 mole percent, and y is from about 10 to about 30 mole percent. 42.The composition as in claim 41 wherein R² is selected from the groupconsisting of ##STR60##
 43. The composition as in claim 39 or 40 whereinthe repeating unit ##STR61## is the condensation residue of adicarboxylic acid selected from the group consisting of3,3'-[(sodioimino)disulfonyl]dibenzoic acid;3,3'-[(potassioimino)disulfonyl]dibenzoic acid;3,3'-[(lithioimino)disulfonyl]dibenzoic acid;4,4'-[(lithioimino)disulfonyl]dibenzoic acid;4,4'-[(sodioimino)disulfonyl]dibenzoic acid;4,4'-[(potassioimino)disulfonyl]dibenzoic acid;3,4'-[(lithioimino)disulfonyl]dibenzoic acid;3,4'-[(sodioimino)disulfonyl]dibenzoic acid;4,4'-[(potassiomino)disulfonyl]dinaphthoic acid;5-[N-potassio-N-(4-tolylsulfonyl)sulfamoyl]isophthalic acid5-sodiosulfoisophthalic acid, 5-(4-sodiosulfophenoxy)isophthalic acid,5-(3-sodiosulfopropoxy)isophthalic acid, and5-(4-sodiosulfocyclohexyloxy)-1,3-cyclohexanedicarboxylic acid.
 44. Anaqueous photoconductive composition as in claim 41 wherein the repeatingunit ##STR62## is the condensation residue of a dicarboxylic acidselected from the group consisting of3,3'-[(sodioimino)disulfonyl]dibenzoic acid;3,3'-[(potassioimino)disulfonyl]dibenzoic acid;3,3'-[(lithioimino)disulfonyl]dibenzoic acid;4,4'-[(lithioimino)disulfonyl]dibenzoic acid;4,4'-[(sodioimino)disulfonyl]dibenzoic acid;4,4'-[(potassioimino)disulfonyl]dibenzoic acid;3,4'-[(lithioimino)disulfonyl]dibenzoic acid;3,4'-[(sodioimino)disulfonyl]dibenzoic acid;4,4'[(potassiomino)disulfonyl]dinaphthoic acid;5-[(N-potassio-N-(4-tolylsulfonyl)sulfamoyl]isophthalic acid5-sodiosulfoisophthalic acid, 5-(4-sodiosulfophenoxy)isophthalic acid,5-(3-sodiosulfopropoxy)isophthalic acid, and5-(4-sodiosulfocyclohexyloxy)-1,3-cyclohexanedicarboxylic acid.